Interfacial redox processes of cytochrome b562

• Autores: Zuo, P.; Albrecht, T.; Barker, P.D.; Murgida, Daniel Horacio; Hildebrandt, P.
• Año de publicación: 2009
• Idioma: inglés
• Tipo de recurso: artículo
• Materia: Citocromos; Transferencia Electrónica; Raman
• Institución: Consejo Nacional de Investigaciones Científicas y Técnicas

The anionic soluble heme protein cytochrome b562 was electrostatically immobilised on Ag electrodes coated with positively charged self-assembled monolayers of amino-terminated alkanethiols. The structure of the heme pocket, the redox equilibria, and the electron transfer dynamics were studied by stationary and time-resolved surface enhanced resonance Raman spectroscopy, complemented by cyclic voltammetry measurements of the interfacial redox process. The conformational and redox equilibria of the immobilised protein are compared to those of the cationic heme protein cytochrome c immobilised on negatively charged electrode coatings. Similarities and differences can be rationalised in terms of the respective electric fields at the interfaces of amino- and carboxyl-terminated electrode coatings. The heterogeneous electron transfer rate of cytochrome b562 only slightly increases with decreasing thickness from ca. 20 to 11 Å, implying that the electron tunneling is not the rate-limiting step. In contrast to cytochrome c on carboxyl-terminated monolayers, this behaviour cannot be attributed to protein re-orientation gating the heterogeneous electron transfer. Instead, it may reflect the interplay between interprotein electron transfer and heterogeneous electron transfer via protein orientations exhibiting particularly high tunneling probabilities for the electron exchange with the electrode.
Fil: Zuo, P.. Technishe Universitat Berlin; Alemania
Fil: Albrecht, T.. Imperial College London; Reino Unido
Fil: Barker, P.D.. University of Cambridge; Reino Unido
Fil: Murgida, Daniel Horacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Inorgánica, Analítica y Química Física; Argentina
Fil: Hildebrandt, P.. Technishe Universitat Berlin; Alemania